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Detecting rare cells within blood has numerous applications in disease diagnostics. Existing rare cell detection techniques are typically hindered by their high cost and low throughput. Here, we present a computational cytometer based on magnetically modulated lensless speckle imaging, which introduces oscillatory motion to the magnetic-bead-conjugated rare cells of interest through a periodic magnetic force and uses lensless time-resolved holographic speckle imaging to rapidly detect the target cells in three dimensions (3D). In addition to using cell-specific antibodies to magnetically label target cells, detection specificity is further enhanced through a deep-learning-based classifier that is based on a densely connected pseudo-3D convolutional neural network (P3D CNN), which automatically detects rare cells of interest based on their spatio-temporal features under a controlled magnetic force. To demonstrate the performance of this technique, we built a high-throughput, compact and cost-effective prototype for detecting MCF7 cancer cells spiked in whole blood samples. Through serial dilution experiments, we quantified the limit of detection (LoD) as 10 cells per millilitre of whole blood, which could be further improved through multiplexing parallel imaging channels within the same instrument. This compact, cost-effective and high-throughput computational cytometer can potentially be used for rare cell detection and quantification in bodily fluids for a variety of biomedical applications.
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http://dx.doi.org/10.1038/s41377-019-0203-5 | DOI Listing |
Opt Express
February 2025
This work presents a computationally efficient transmission matrix model and optimization scheme for the design of silicon nitride grating couplers in integrated scattering-based flow cytometry systems. The proposed model accurately simulates the optical power flow through the grating coupler and microfluidic channel system, enabling precise evaluation of the transient associated with a polystyrene bead's passage through the channel. The transmission matrix model yields a four to five orders-of-magnitude improvement in computational efficiency compared to a finite difference time domain solver, making it suitable for optimization loops consisting of many iterations and objective function evaluations.
View Article and Find Full Text PDFCytometry A
August 2025
Microsystems and Nanotechnology Division, National Institute of Standards and Technology, Gaithersburg, Maryland, USA.
Flow cytometers are powerful tools for bioanalytical applications, yet new systems that promise better measurements are continuously being introduced as sensors and other technologies advance. One such advancement by NIST was the recently demonstrated a serial microcytometer that enables unique capabilities for uncertainty quantification on a per-object basis. In an effort to benchmark and improve the measurement capabilities of the serial microcytometer, we found limitations to the quantitative comparison of instruments using conventional metrics and methods.
View Article and Find Full Text PDFTheriogenology
December 2025
Departamento de Ciencias Veterinarias, Instituto de Ciencias Biomédicas, Universidad Autónoma de Ciudad Juárez, Ciudad Juárez, Chihuahua, 32310, México. Electronic address:
Cryopreservation induces negative effects on spermatozoa due to oxidative stress. The aim of this study was to evaluate the effect of the addition of quercetin and gallic acid on sperm characteristics under the cryopreservation process of domestic dog epididymal semen. Samples were collected from sexually mature males by direct epididymal collection technique after orchiectomy and diluted with a commercial extender.
View Article and Find Full Text PDFFront Vet Sci
July 2025
Animal Physiology and Reproduction Division, ICAR-Central Institute for Research on Buffaloes, Hisar, Haryana, India.
For cattle bulls, only ejaculates with a sperm concentration of 500 million/mL or higher are selected for sperm cryopreservation. There is no established ejaculate's minimum sperm concentration threshold for buffalo semen cryopreservation. Therefore, the first objective of the study was to determine the percentage of ejaculates of buffalo bulls having concentrations lower than 500 million/mL, the percentage of ejaculates suitable for cryopreservation across different concentrations of donated ejaculates, and to estimate the impact of ejaculate concentrations on the production of semen doses.
View Article and Find Full Text PDFTalanta
January 2026
Henan Key Laboratory of Diamond Optoelectronic Materials and Devices, Key Laboratory of Materials Physics, Ministry of Education, School of Physics, Zhengzhou University, Zhengzhou, 450001, China.
Imaging flow cytometry is a widely used technique for high-throughput, label-free single-cell analysis. However, its effectiveness is often compromised by experimental perturbations, such as random defocusing and off-axis light coupling, which degrade image quality and hinder reliable analysis. In this study, we present a robust imaging flow cytometer based on in-silico optofluidic time-stretch imaging with the assistance of optical phase.
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